What is an EU Declaration of Conformity?

The CE mark is a mandatory European marking for machinery and equipment to indicate conformity with the essential health and safety requirements set out in ... Transparency and Safety on European Markets. CE Marking. Only safe, flawless, and quality goods should be available on the European market – at least, that's ... 7 Steps to CE Certification with Intertek · Determine which directive(s) are applicable to your product · Fulfill the essential requirements · Establish a ... What the CE mark means. The CE mark is proof that the product meets basic safety requirements. The brand says nothing about the quality of the product. What ... CE marking is required for all in vitro diagnostic (IVD) devices sold in Europe. CE marking indicates that an IVD device complies with the European In-Vitro ... We are regulatory professionals who guide on specific requirements that must be met and obtain the medical device CE Marking. Manufacturers can place a CE (Conformité Européenne) mark on a medical device once it has passed a conformity assessment. The conformity assessment usually ... The "CE" marking is a European logo indicating that the manufacturer has complied with certain compliance requirements to which the product is subject, to put ... CE marking is a self-declaration where a manufacturer proves compliance with EU health, safety and environmental protection legislation and confirms a product's ... Jun 10, 2024 ... CE marking is a manufacturer's declaration that a product meets the requirements of the applicable European Community directives.